FDA Inspection 781222 — Medtronic Monitoring Inc.

Medtronic Monitoring Inc. — FEI 3007456577

The FDA completed an inspection of Medtronic Monitoring Inc. on May 22, 2012 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 22, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)